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The aim of the study is to evaluate the adverse events and the efficacy of virus specific T lymphocytes selected in vitro from a family donor to treat some refractory viral infections as Adenovirus (ADV), Ebstein Barr virus (EBV), Cytomegalovirus (CMV) that developed in young patients (age between 0 and 21 years) after allogeneic hematopoietic cell transplantation (allo-HSCT) performed at the Transplant Clinical Unit of the IRCCS G. Gaslini Institute (IGG).
The rationale for the study is based on the evidence that, despite the progress obtained in the management and prevention of viral infections in the patients who received allo-HSCT, some viral infections continue to be severe complications that may occurred before the immune recovery. Some of these viral reactivations are not responsive to the first or second line treatment and their treatment may be represent an important issue. The adoptive cellular immunotherapy based on the infusion of virus-specific T lymphocytes represent a valid therapeutic option and the quick access to this cellular therapy is crucial to prevent severe organ complications related to viral infection. In this study, the use of virus-specific T lymphocytes obtained from a seropositive family donor, briefly activated in vitro and immunomagnetically captured by their capacity to secrete IFN-gamma allows to obtain a rapidly usable T-lymphocyte population (both CD4+ and CD8+) potentially able to expand into the patient. The effectiveness, safety (peptides used are synthetic, no animal components, closed system production), good tolerance and speed of modality (less than 36 hours for production) is reported by many clinical studies.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Virus-specific T cells for the treatment of active viral infections following allogeneic HSCT. | Experimental | Virus specific T lymphocytes selected in vitro from a family donor to treat some refractory viral infections as Adenovirus (ADV), Ebstein Barr virus (EBV), Cytomegalovirus (CMV) that developed in young patients (age between 0 and 21 years) after allogeneic hematopoietic cell transplantation (allo-HSCT) |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Virus -specific T cells | Biological | The product is obtained by leukapheresis of a family donor responsive to the virus: consists of virus- specific T lymphocytes (both CD4+ and CD8+) resuspended in PBS / EDTA buffer plus 0.5% Albumin Human. The productive process lasts two consecutive days and includes two phases: a brief activation with specific viral peptide followed by immunomagnetic separation using the CliniMACS® CCS (IFNγ) capture system which allows a fast and automated separation of IFNγ secreting lymphocytes |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | To collect any adverse event defined as any significant alteration of vital signs and / or organ function, expressed in clinical, hematochemical and radiological findings according to version 5 of the Common Terminology Criteria for Adverse Events (CTCAE) | from day +1 of infusion until day +56 |
| Measure | Description | Time Frame |
|---|---|---|
| Specific cell viral immunity | To evaluate the specific cell viral immunity for some virus defined as presence and number of CD3 + IFN-gamma + lymphocytes count in the patient's peripheral blood | from day +1 of infusion until day +56 |
| Variation of viremia |
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Inclusion criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Maura Faraci, MD | Contact | 01056362405 | maurafaraci@gaslini.org | |
| Stefano Giardino, MD | Contact | 01056362405 | stefanogiardino@gaslini.org |
| Name | Affiliation | Role |
|---|---|---|
| Maura Faraci, MD | Istituto G. Gaslini | Principal Investigator |
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IPD are to be shared with hematologists and oncologists of our Institute
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| ID | Term |
|---|---|
| D000257 | Adenoviridae Infections |
| ID | Term |
|---|---|
| D004266 | DNA Virus Infections |
| D014777 | Virus Diseases |
| D007239 | Infections |
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Phase I, open-label, single-arm, non-randomized study, monocentric.
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To evaluate viremia variations with the measurement of viral PCR after the infusion of virus-specific T lymphocytes evaluated regularly 2 times a week. |
| from day +1 of infusion until day +56 |
| Organ damage | To report any clinical and/or laboratory changes related to the viral infection | from day +1 of infusion until day +56 |
| Overall survival | To evaluate the overall survival (OS) after virus-specific T lymphocytes | from day +56 to 12 months |